SUPRAX
- Product NDC
- 27437-207
- 11-digit product format
- 274370207
- Labeler code
- 27437
- Product ID
- 27437-207_0e44b51b-cba9-4dc5-8ee1-2d151ad24def
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- cefixime
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Lupin Pharmaceuticals, Inc.
- Application
- NDA202091
- Marketing category
- NDA
- Marketing start
- 2013-03-15
- Marketing end
- 0000-00-00
- Substance
- CEFIXIME
- Active strength
- 500 mg/5mL
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 27437-207-02 | 27437020702 | 10 mL in 1 BOTTLE (27437-207-02) | 10 ml | 2013-03-15 | 0000-00-00 | No | No | Current |
| 27437-207-03 | 27437020703 | 20 mL in 1 BOTTLE (27437-207-03) | 20 ml | 2013-03-15 | 0000-00-00 | No | No | Current |
| 27437-207-04 | 27437020704 | 1 BOTTLE in 1 CARTON (27437-207-04) > 10 mL in 1 BOTTLE | 1 bottle | 2013-03-15 | 0000-00-00 | No | No | Current |